Wiggs W J, Sismanis A, Laine F J
Department of Otolaryngology-Head and Neck Surgery, Medical College of Virginia, Richmond 23298, USA.
Am J Otol. 1996 Mar;17(2):241-4.
Pulsatile tinnitus as a manifestation of congenital central nervous system malformations has not been previously described. We present two patients with type I Arnold-Chiari malformation and one patient with congenital stenosis of the sylvian aqueduct with pulsatile tinnitus. Pulsatile tinnitus in these patients is believed to be secondary to increased intracranial pressure. Tinnitus subsided in one patient with Arnold-Chiari malformation after suboccipital decompression. The other two patients declined surgery. Audiologic and radiologic findings are presented, and our diagnostic algorithm for pulsatile tinnitus is described. The pathophysiology of pulsatile tinnitus can be a manifesting symptom in some patients with congenital central nervous system malformations.
搏动性耳鸣作为先天性中枢神经系统畸形的一种表现,此前尚未见报道。我们报告了2例Ⅰ型阿诺德-基亚里畸形患者和1例伴有搏动性耳鸣的先天性大脑导水管狭窄患者。这些患者的搏动性耳鸣被认为是颅内压升高所致。1例阿诺德-基亚里畸形患者在枕下减压术后耳鸣消失。另外2例患者拒绝手术。本文展示了听力学和放射学检查结果,并描述了我们针对搏动性耳鸣的诊断算法。搏动性耳鸣的病理生理学在一些先天性中枢神经系统畸形患者中可能是一种表现症状。